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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243823Generated: October 31, 2026

Cyclopropylamine → (N-cyclopropyl)-6,6-diphenyl-6,7-dihydro-1H-indazole-3-carboxamide

https://huagongshe.com/reaction/1243823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant6,6-diphenyl-6,7-dihydro-1H-indazole-3-carboxylic acidHCID 21928673—
ReactantHCID 178418300HCID 178418300—
SolventDichloromethaneHCID 6344—
Product(N-cyclopropyl)-6,6-diphenyl-6,7-dihydro-1H-indazole-3-carboxamideHCID 21929970—

Reaction Conditions

Temperature20 °C

Reaction Steps

Starting with a mixture of 1.23 g of 6,6-diphenyl-6,7-dihydro-1H-indazole-3-carboxylic acid, 0.26 cm3 of cyclopropylamine, 0.86 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride and 60 mg of hydroxybenzotriazole in solution in 30 cm3 of dichloromethane, and after stirring for 18 hours at a temperature in the region of 20° C., washing with twice 30 cm3 of distilled water and purifying the crude product obtained by flash chromatography on silica gel (30–70 μm), eluting with a cyclohexane/ethyl acetate (60/40) mixture, 0.58 g of (N-cyclopropyl)-6,6-diphenyl-6,7-dihydro-1H-indazole-3-carboxamide is obtained in the form of a yellow solid, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119115B2
Source datasetuspto-grants-2006_10
ORD IDord-677c95aaa1d742788d93011560fa819f
Source noteuspto-grants-2006_10